A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576296



Internal ID21768339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171404170..171404254hg38UCSC Ensembl
chr5:170831174..170831258hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011730
Supporting Variants
Samples
Known GenesNPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576296
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer